Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Dingli Chen"'
Autor:
Shouxia Li, Shurui Li, Dingli Chen, Subin Zhao, Cairu Liu, Ruimin Zhang, Yongxue Chen, Xiangrui Guo, Xuedong Song
Publikováno v:
Medicine; 4/19/2024, Vol. 103 Issue 16, p1-7, 7p
Autor:
Renjie Cui, Dingli Chen, Na Li, Ming Cai, Teng Wan, Xueqiang Zhang, Meiqin Zhang, Sichen Du, Huayuan Ou, Jianjun Jiao, Nan Jiang, Shuangxia Zhao, Huaidong Song, Xuedong Song, Duan Ma, Jin Zhang, Shouxia Li
Publikováno v:
Journal of Cellular and Molecular Medicine. 26:4292-4304
Nonsyndromic cleft palate only (NSCP) is a common congenital malformation worldwide. In this study, we report a three-generation pedigree with NSCP following the autosomal-dominant pattern. Whole-exome sequencing and Sanger sequencing revealed that o
Autor:
Cong Huang, Qiang Lin, Shaokang Peng, Zheng Xu, Min Zhang, Dingli Chen, Haoming Sun, Jizhao Chen, Lei Miao, Zongping Wang
Publikováno v:
Desalination & Water Treatment; May2023, Vol. 295, p125-132, 8p
Publikováno v:
Biomarkers in medicine. 15(14)
Autor:
Xuedong Song, Lili Guo, Dingli Chen, Shouxia Li, Caixia Sun, Shurui Li, Su-Bin Zhao, Xiaofang Zhang
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 136:110172
Waardenburg Syndrome (WS) is a condition characterized by sensorineural deafness and pigment disturbances of the skin, hair and iris. By using the latest genomics technology, the WS-related gene mutations and corresponding mechanisms have been widely
Autor:
Jin Zhang, Xiaofang Zhang, Sujun Yang, Duan Ma, Gendong Yao, Shouxia Li, Dingli Chen, Zhiming Yang, Caixia Sun, Zhixing Feng, Lili Guo, Huijun Wang
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 77:544-549
Objective Enlarged vestibular aqueduct is the most common inner ear malformation in individuals with sensorineural hearing loss. Mutations in SLC26A4 can cause non-syndromic EVA. To date, more than 170 SLC26A4 mutations have been described. The aim o
Autor:
Xueqiang Zhang, Xuedong Song, Shouxia Li, Dingli Chen, Caixia Sun, Wei Zhao, Chun Liang, Lei Yin, Lili Guo, Xiaofang Zhang, Jianjun Jiao
Publikováno v:
Molecular medicine reports. 17(1)
Members from two Van der Woude syndrome (VWS) families were screened to determine the prevalence of interferon regulatory factor 6 (IRF6) as a disease‑causing gene and to analyze the interrelationships between patient genotype and phenotype. The pe
Autor:
Lili Guo, Xiaofang Zhang, Huijun Wang, Shouxia Li, Jin Zhang, Zhixing Feng, Sujun Yang, Duan Ma, Gendong Yao, Dingli Chen, Zhiming Yang, Caixia Sun
Publikováno v:
Acta oto-laryngologica. 133(8)
This study demonstrated high prevalence of GJB2, SLC26A4, and mtDNA A1555G mutations in Chinese patients with nonsyndromic hearing loss and discovered eight novel mutations in SLC26A4. Most of these novel mutations were predicted pathogenic variants.
Publikováno v:
Publications of the Astronomical Society of the Pacific. 107:667
We report BVRI photometry of stars in 12 selected extreme ultraviolet ROSAT fields with the goal of obtaining firm identifications of the optical counterparts to the ROSAT sources. We present BVRI magnitudes and finder charts for 10 optical counterpa